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Methods for Adeno-Associated Viral Vector Production

a technology of adenovirus and vector production, which is applied in the field of nuclear acid vectors, can solve the problems of difficult to completely remove the adenovirus from the aav product, high labor intensity and high cost of the process, and achieve the effect of easing problems

Active Publication Date: 2018-11-15
GLAXOSMITHKLINE INTPROP DEV LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

This patent describes a new way of making packaging and producer cell lines for adeno-associated virus (AAV) vectors. The inventors used nucleic acid vectors containing a non-mammalian origin of replication and the ability to hold at least 25 kilobases of DNA. This allows for the integration of all the AAV genes required for vector production, as well as a selective antibiotic resistance gene, into the producer cell genome. This approach has several advantages, including easier manipulation in non-mammalian cells, faster screening of potential packaging cells, and reduced cost of materials and testing. Additionally, the use of these vectors allows for the integration of all the required genes at one locus within the host cell genome, reducing the likelihood of gene silencing. Overall, this patent provides a better way to generate packaging and producer cell lines for AAV vectors.

Problems solved by technology

Furthermore, AAV is not currently known to cause disease and therefore causes little to no toxicity and inflammation in vivo.
Although this method has been shown to be easily scaled up in cultures and produce AAV vectors with high titres, it is very challenging to completely remove the adenovirus from the AAV product.
Contamination of wildtype adenovirus is highly undesirable in view of vector safety and specificity.
Although this transient transfection method generates high titres of AAV vectors that are free of adenovirus, the process is very labour-intensive and expensive.

Method used

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  • Methods for Adeno-Associated Viral Vector Production
  • Methods for Adeno-Associated Viral Vector Production
  • Methods for Adeno-Associated Viral Vector Production

Examples

Experimental program
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example 1

AAV Bacterial Artificial Chromosome

[0213]Nucleic acid vectors of the invention may be designed using methods known in the art. A detailed, exemplary method is provided herein:

[0214]Gibson cloning primers are designed to amplify the tetracycline-controlled transactivator (tTA) gene in a construct including a PCMV promoter, an IRES, and a Zeocin resistance gene in the order PCMV-intron-tTA-ZeoR-polyA. The primers allow cloning into the pSMART BAC backbone (Lucigen Corp.) by Gibson assembly. A restriction site for PI-PspI for sequential iBrick cloning (Liu et al. (2014) PLoS One 9(10):e110852, incorporated herein by reference) is included between the polyA and the plasmid.

[0215]Two chicken HS4 (cHS4) insulators in tandem are cloned 3′ of the ZeoR polyA into the PI-PspI site as follows. The 2×cHS4 fragment from pMA-BACmod-GSKCOTR-IR-Zeo is amplified using I-SceI forward and PI-PspI reverse primers. Between the I-SceI site and the 2×cHS4 insulators are restriction sites for MluI and NheI...

example 2

d Synthesis of AAV BAC with Additional Components

[0221]A BAC was created containing every genetic element (i.e. expression cassettes) required for rAAV particle production cloned into it: the AAV rep / cap gene; the helper virus genes and a recombinant DNA genome of an AAV vector particle. Furthermore, additional components were also included as outlined below.

[0222]In order to control the level of AAV Rep expressed in the transfected mammalian cell, it was decided to include shRNA targeting Rep and E1A in the construct under the control of a conditional promoter (Ptet-T6).

[0223]The BAC also includes the tetracyclin-sensitive transcriptional activator, tTA. Under normal growth conditions, suspension adapted HEK293 cells in which the construct is stably integrated into the genome would express the shRNA and Rep and E1A expression would be knocked down. When the cells reached a density suitable for rAAV particle production, doxycycline (DOX) could be added to the growth medium. This wou...

example 3

n of AAV Stable Producer Cell Line (Suspension Cells)

[0322]A stable cell line was established by transfecting AdVec 293 suspension cells with BAC9a-GFP. As a transient transfection control, the AdVec 293 cells were also co-transfected with a rep / cap plasmid, a helper plasmid (carrying helper genes from adenovirus) and pG.AAV.CMV.GFP.P2A.fluc.W6 (transfer vector with ITR flanking GFP transgene) at a 1:1:1 ratio based on molar ratios.

3.1 AdVec 293 RS-D01 Suspension Cells

[0323]AdVec suspension cells were maintained in BalanCD media (with 2% GlutaMAX and 1% Pluronic F-68) at 0.4×106 cell / ml and split every 2-3 days. Cells are incubated 37° C., 5% CO2, 110 rpm. Small scale cultures were maintained at higher rotation (140 rpm) to aid aeration.

3.2 Transfection of AdVec 293 RS-D01 Suspension Cells

[0324]Prior to transfection, cells were centrifuged at 500 rpm for 10 min at 4° C., the supernatant removed and the cell pellet resuspended in fresh pre-warmed BalanCD media, counted and seeded at ...

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Abstract

The invention relates to an adeno-associated virus (AAV) producer cell comprising nucleic acid sequences encoding: rep / cap gene; helper virus genes; and the DNA genome of the AAV vector particle, wherein the nucleic acid sequences are all integrated together at a single locus within the AAV producer cell genome. The invention also relates to nucleic acid vectors comprising a non-mammalian origin of replication and the ability to hold at least 25 kilobases (kb) of DNA, characterized in that the nucleic acid vectors comprise nucleic acid sequences encoding: rep / cap gene, and helper virus genes. The invention also relates to uses and methods using the nucleic acid vectors in order to produce stable AAV packaging and producer cell lines.

Description

CROSS REFERENCE TO RELATED APPLICATION[0001]This application claims the benefit of U.K. Provisional Application No. 1706090.6, filed on Apr. 18, 2017.FIELD OF THE INVENTION[0002]The invention relates to nucleic acid vectors comprising genes required for adeno-associated viral (AAV) vector production and uses thereof. Also provided are methods of making AAV packaging and producer cell lines comprising the nucleic acid vectors as described herein.BACKGROUND TO THE INVENTION[0003]In gene therapy, genetic material is delivered to endogenous cells in a subject in need of treatment. The genetic material may introduce novel genes to the subject, or introduce additional copies of pre-existing genes, or introduce the wild type variant of genes that are defective in the subject. Viral vector systems have been proposed as an effective gene delivery method for use in gene therapy (Verma and Somia (1997) Nature 389: 239-242).[0004]Adeno-associated virus (AAV) was discovered in 1965, as a contami...

Claims

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Application Information

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IPC IPC(8): C12N7/00
CPCC12N7/00C12N2750/14152C12N2750/14121C12N15/86C12N2750/14143C07K14/005C12N2710/10322C12N15/861
Inventor VINK, CONRAD
Owner GLAXOSMITHKLINE INTPROP DEV LTD
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